(FC) Bioquímica y Genética
Departamento académico
Ana Isabel
Heiniger Mazo
Publicaciones en las que colabora con Ana Isabel Heiniger Mazo (13)
2009
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Epigenetic regulation of MicroRNAs in acute lymphoblastic leukemia
Journal of Clinical Oncology, Vol. 27, Núm. 8, pp. 1316-1322
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Epigenetic silencing of the tumor suppressor microRNA Hsa-miR-124a regulates CDK6 expression and confers a poor prognosis in acute lymphoblastic leukemia
Cancer Research, Vol. 69, Núm. 10, pp. 4443-4453
2008
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BCR-ABL1-induced expression of HSPA8 promotes cell survival in chronic myeloid leukaemia
British Journal of Haematology, Vol. 142, Núm. 4, pp. 571-582
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Down-regulation of hsa-miR-10a in chronic myeloid leukemia CD34+ cells increases USF2-mediated cell growth
Molecular Cancer Research, Vol. 6, Núm. 12, pp. 1830-1840
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Resistance to Imatinib Mesylate-induced apoptosis in acute lymphoblastic leukemia is associated with PTEN down-regulation due to promoter hypermethylation
Leukemia Research, Vol. 32, Núm. 5, pp. 709-716
2007
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Epigenetic regulation of Wnt-signaling pathway in acute lymphoblastic leukemia
Blood, Vol. 109, Núm. 8, pp. 3462-3469
2006
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ASPP1, a common activator of TP53, is inactivated by aberrant methylation of its promoter in acute lymphoblastic leukemia
Oncogene, Vol. 25, Núm. 13, pp. 1862-1870
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Abnormal methylation of the common PARK2 and PACRG promoter is associated with downregulation of gene expression in acute lymphoblastic leukemia and chronic myeloid leukemia
International Journal of Cancer, Vol. 118, Núm. 8, pp. 1945-1953
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CpG island methylator phenotype redefines the prognostic effect of t(12;21) in childhood acute lymphoblastic leukemia
Clinical Cancer Research, Vol. 12, Núm. 16, pp. 4845-4850
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Downregulation of DBC1 expression in acute lymphoblastic leukaemia is mediated by aberrant methylation of its promoter
British Journal of Haematology, Vol. 134, Núm. 2, pp. 137-144
2004
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Promoter hypermethylation of cancer-related genes: A strong independent prognostic factor in acute lymphoblastic leukemia
Blood, Vol. 104, Núm. 8, pp. 2492-2498